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Clinical Trials/NCT01789229
NCT01789229
Recruiting
Not Applicable

Establishment of a Tissue Sample Bank in the Field of Gynaecological Oncology

Medical University of Vienna3 sites in 3 countries10,000 target enrollmentSeptember 2003

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ovarian Neoplasms
Sponsor
Medical University of Vienna
Enrollment
10000
Locations
3
Primary Endpoint
Establishment of blood/tissue bank consisting of oncological samples from cancer patients and benign and healthy controls.
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Establishment of a tumor bank, consisting of tissue samples of tumor patients (benign and malign tumors) and healthy people as controls. The tissue samples will be collected systematically together with the corresponding clinical data. The biological samples, the clinical date together with prospective experimental date constitute the entity of the tissue tumor bank.

This tumor bank for tissue samples, together with our tumorbank for blood samples (NCT01763125) combined constitute the entity "Tumorbank".

Detailed Description

Recent progress in diagnosis and therapy of cancer diseases can be ascribed mainly to translational research. The relevance of "translational oncology" will only increase in the future -"From bench to bedside" - the swift implementation of new science research results in clinical studies in order to expedite progress in clinical cancer therapy for the benefit of the patient. Its almost a matter of course in the medical science today to collect biological samples together with clinical information thereby creating the foundation for future excellent fundamental research. The aim of this tumor bank is to consist of biological samples (together with a blood bank - see NCT01763125) and isolates of tumor patients and healthy people as controls. The biological samples, the clinical date together with prospective experimental date constitute the entity of the tumor bank. The content of the tumor bank can provide essential material for current and future research (e.g. analyses of prognostic or predictive tumor markers; genetically analysis (polymorphism, mutation, hypermethylation; verification and characterisation of disseminated tumor cells).

Registry
clinicaltrials.gov
Start Date
September 2003
End Date
December 2026
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Robert Zeillinger, Dr.phil.

Univ.Prof. Dr.

Medical University of Vienna

Eligibility Criteria

Inclusion Criteria

  • Male/Female
  • Age 18 to 90 years max.
  • Just one current known malignant disease or just one current inflammatory disease

Exclusion Criteria

  • Inflammatory disease and malignant disease
  • multiple malignancies
  • multiple diseases

Outcomes

Primary Outcomes

Establishment of blood/tissue bank consisting of oncological samples from cancer patients and benign and healthy controls.

Time Frame: 14 years

Study Sites (3)

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